A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975235



Internal ID22750170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90664119..90686002hg38UCSC Ensembl
chr5:89959936..89981819hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3821884
hg1921884
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422749
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975235
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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